510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
NCFClass I

Aberrometer, Ophthalmic

21 CFR 886.1760 / Ophthalmic
FDA source (opens on fda.gov)

NCF is the FDA product code for Aberrometer, Ophthalmic, a class I device type, regulated under 21 CFR 886.1760. As of , FDA records hold 4 510(k) clearances under this code, the most recent dated , and 2 recalls.

Classification record

Product code
NCF
Device name
Aberrometer, Ophthalmic
Regulation
21 CFR 886.1760
Device class
Class I
Review panel
Ophthalmic
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
4
Ingested recalls
2

Clearances, product code NCF

By decision year
4 clearances under product code NCF with a decision year between 2000 and 2006, 2000 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code NCF by decision year
YearClearances
20001
20021
20051
20061

Applicants with the most clearances

Product code NCF
Applicants holding the most 510(k) clearances under product code NCF
ApplicantClearances
Alcon Laboratories3
Nidek, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code